摘要
将首尾带有EcoRI酶切位点的 2 .0kb、1.5kb、1.0kb、0 .75kb、0 .5kb、0 .2 5kb六个长度的片段逐步连接到pGEM - 3zf(+)质粒上的BamHI位点中 ,构建的质粒用EcoRI进行单酶切 ,经电泳可以获得七条DNA带与设计结果完全一致 ,可用于DNA电泳试验中分子量标准。
Six fragments 2.0kb,1.5kb,1.0kb,0.75kb,0.5kb,0.25kb,which have two EcoR I restriction enzyme sites in each end side of them were recombined into BamH I restriction enzyme sites of pGEM-3zf(+) plasmid one by one.The restriction analysis demonstrated that the marker vector had been recombined.It can be use as DNA marker and will be very useful for the biotechnology lab.
出处
《生物技术》
CAS
CSCD
2004年第5期33-35,共3页
Biotechnology